Department of Physical Chemistry II, Ruhr University Bochum, Bochum, Germany.
Current affiliation: Department of Chemistry "U. Schiff", University of Florence, I-50019, Sesto Fiorentino, FI, Italy.
Angew Chem Int Ed Engl. 2022 Jul 18;61(29):e202203893. doi: 10.1002/anie.202203893. Epub 2022 Jun 1.
Hydration free energies are dictated by a subtle balance of hydrophobic and hydrophilic interactions. We present here a spectroscopic approach, which gives direct access to the two main contributions: Using THz-spectroscopy to probe the frequency range of the intermolecular stretch (150-200 cm ) and the hindered rotations (450-600 cm ), the local contributions due to cavity formation and hydrophilic interactions can be traced back. We show that via THz calorimetry these fingerprints can be correlated 1 : 1 with the group specific solvation entropy and enthalpy. This allows to deduce separately the hydrophobic (i.e. cavity formation) and hydrophilic contributions to thermodynamics, as shown for hydrated alcohols as a case study. Accompanying molecular dynamics simulations quantitatively support our experimental results. In the future our approach will allow to dissect hydration contributions in inhomogeneous mixtures and under non-equilibrium conditions.
水合自由能是由疏水性和亲水性相互作用的微妙平衡决定的。我们在这里提出了一种光谱方法,可以直接研究两个主要贡献:使用太赫兹光谱来探测分子间拉伸(150-200cm)和受阻旋转(450-600cm)的频率范围,可以追溯到由于腔形成和亲水相互作用引起的局部贡献。我们表明,通过太赫兹量热法,这些指纹可以与特定基团的溶剂化熵和焓一一相关。这允许分别推断疏水(即腔形成)和亲水对热力学的贡献,如以水合醇作为案例研究所示。伴随的分子动力学模拟定量支持我们的实验结果。在未来,我们的方法将允许在非均匀混合物和非平衡条件下剖析水合作用的贡献。